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Completed

NCT Number: NCT03589716

Evaluating the Accuracy of an Integrated Vital Sign Measurement Platform

Partners Connected Health will conduct a clinical validation study to evaluate the accuracy of measurement for each vital sign with the Vital Moto Mod platform, compared to appropriate reference devices used in the hospital setting. The study will recruit volunteers from the Partners Healthcare network of clinics and hospitals and the general public.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Partners Connected Health

Boston, Massachusetts, 02114, United States

About this study

To assess the comparative clinical performance of the Vital Moto Mod device in the measurement of five vital signs (body temperature, respiratory rate, heart rate, oxygen saturation and blood pressure) in correlation with a reference device used in the hospital environment for vital sign measurement.

Vital sign measurement is a core process in delivering healthcare. Body temperature, respiratory rate, heart rate, oxygen saturation and blood pressure are some of the most frequently measured vital signs in inpatient as well as outpatient encounters. Currently, separate devices exist for measurement of each of these vital signs, each of which may have to be measured several times in a day. Consequently, measurement of vital signs is a time and human resource intensive process. Moreover, most of the devices currently used to measure vital signs cannot transmit data to the electronic medical record of patient, thereby creating opportunities for human error. VVVital USA has used proprietary sensor technology to develop Vital Moto Mod - a vital sign measurement platform that can non-invasively measure body temperature, respiratory rate, heart rate, oxygen saturation and blood pressure from a person's index finger, and allows this information to be pushed into their electronic medical/health record from the point of care

The primary market focus use of the Vital Moto Mod is to replace the vital sign cart in hospitals. Vital sign carts are expensive and cumbersome to move around the hospital. At a fraction of the cost, the Vital Moto Mod provides the same functionality including bar code scanning at a fraction of the cost. Additionally, the Vital Moto Mod can also be used at home without the need for a trained nurse. The Vital Moto Mod App will guide a user through the workflow of performing the measurements. The Vital Moto Mod is connected to a smartphone for storage, and has a USB interface for charging, thereby requiring no electrical connections during use. All measurements are taken by the device independent of the phone.

Partners Connected Health will conduct a clinical validation study to evaluate the accuracy of measurement for each vital sign with the Vital Moto Mod platform, compared to appropriate reference devices used in the hospital setting. The study will recruit volunteers from the Partners Healthcare network of clinics and hospitals and the general public.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

For volunteers with one or more vital signs presumed to be within normal physiological range, at rest:

  • Age ≥ 18 years
  • Willing to allow arm and finger size to be measured
  • Willing to allow measurement of skin color (optional)a
  • Willing to undergo exercise testing (optional);
  • Willing to allow an arterial blood gas draw (optional);

For volunteers with one or more vital signs expected to be outside of normal physiological range, at rest:

  • Age≥18 years
  • Willing to allow arm and finger size to be measured
  • Willing to allow measurement of skin color (optional)

Exclusion criteria

For Volunteers Undergoing Heart Rate and Oxygen Saturation Measurement:

  • Nail paint or artificial nail on the index finger of the left hand
  • SpO2 less than 94%

For Volunteers Undergoing Exercise Testing with Vital Signs within Normal Physiological Range, at rest:

  • Volunteers with vital signs outside of normal physiological range (ascertained during measurements conducted at study site before exercise testing)
  • Age 65 years or older
  • Consumption of food, alcohol or caffeine (coffee, tea or caffeinated soft-drinks) in a 3-hour period prior to testing
  • Uncomfortable clothing, or inappropriate footwear for exercise testing
  • Self-report of any of the following:
  • History of fall or fracture in the past year
  • History of arthritis
  • History of dizziness
  • History of neurological illness
  • History of chest pain or myocardial infarction
  • History of hypertension or diabetes mellitus
  • History of heart disease
  • History of stroke or transient ischemic attack
  • Active treatment for anemia, electrolyte imbalance, or hyperthyroidism
  • Physical disability that precludes safe and adequate testing
  • Mental impairment with limited ability to cooperate4
  • Pregnancy (Volunteer will be excluded if either of the following is true: a) self-report of being pregnant; b) positive urine pregnancy test)

For Volunteers undergoing an Arterial Blood Gas Draw with Vital Signs within Normal Physiological Range, at rest:

  • Self-reported history of a clotting disorder of the blood, or active treatment with medicines affecting blood clotting (e.g. Warfarin).

Treatment and study plan

Vital Moto Mod

Other

All participants receive vital signs measurement using the Vital Moto Mod device and reference devices. The vital signs measured are blood pressure, heart rate, respiratory rate, oxygen saturation and temperature.

Welch Allyn Connex Spot Vital Signs Monitor

Other

This is the FDA approved reference device to measure heart rate, SpO2 and temperature.

Capnostream 20 Portable Bedside Capnograph

Other

This is the reference device to be used to obtain etCO2 waveforms for respiratory rate assessment.

Welch Allyn 767 Mobile Aneroid Sphygmomanometerand 3M Littmann Master Classic II Teaching Stethoscope

Other

These reference devices will be used together for blood pressure measurements.

Scifit 1000R cycle ergometer

Other

This is the device that will be used for exercise testing

Primary outcomes

  1. Number of Vital Moto Mod vital signs measurements in agreement with reference device vital signs measurements

    Time frame: 1 day

    Vital signs measurements for each participant would be compared using the Vital Moto Mod and reference devices for blood pressure, heart rate, respiratory rate, oxygen saturation and temperature

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Vital USA, Inc.

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Jul 18, 2018
Registry last updated
Sep 1, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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